documents: FDA-2013-N-0093-0011

Regulatory documents from Regulations.gov including rules, proposed rules, notices, and supporting materials.

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id agency_id docket_id title document_type subtype posted_date posted_year posted_month comment_start_date comment_end_date last_modified fr_doc_num open_for_comment withdrawn object_id
FDA-2013-N-0093-0011 FDA FDA-2013-N-0093 Agency Information Collection Activities; Proposed Collection; Comment Request; Review Transparency and Communication in Reviews of 351(k) Biologics License Applications in Biosimilars User Fee Act Notice 60 Day Proposed Information Collection 2019-03-12T04:00:00Z 2019 3 2019-03-12T04:00:00Z 2019-05-14T03:59:59Z 2019-07-29T17:42:10Z 2019-04429 0 0 0900006483ad6852

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